- Trials with a EudraCT protocol (134)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (30)
134 result(s) found for: hypothyroidism.
Displaying page 4 of 7.
EudraCT Number: 2014-000178-20 | Sponsor Protocol Number: MCT8-2014-1 | Start Date*: 2015-08-12 |
Sponsor Name:Erasmus Medical Centre | ||
Full Title: Thyroid hormone analog therapy of patients with severe psychomotor retardation caused by mutations in the MCT8 thyroid hormone transporter: The Triac Trial. | ||
Medical condition: This therapuetical trial will be conducted in patient with the Allan-Herndon-Dudley Syndrome (AHDS), casued by mutations in the thyroid hormone transporter MCT8. This results in the characteristic ... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male | |
Trial protocol: BE (Completed) CZ (Completed) DE (Completed) IT (Completed) FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-003175-45 | Sponsor Protocol Number: TRIO 016 | Start Date*: 2009-01-12 | |||||||||||
Sponsor Name:Cancer International Research Group | |||||||||||||
Full Title: A randomized phase II, open-label multicenter trial of panobinostat monotherapy in women with HER2 positive locally recurrent or metastatic breast cancer | |||||||||||||
Medical condition: HER-2 positive locally recurrent or metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001909-77 | Sponsor Protocol Number: VAC18193RSV3006 | Start Date*: 2021-09-22 | |||||||||||
Sponsor Name:Janssen Vaccines & Prevention B.V. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Phase 3 Study to Evaluate the Safety and Immunogenicity of an Ad26.RSV.preF-based Vaccine in Adults Aged 18 to 59Years, Including Those at High-risk f... | |||||||||||||
Medical condition: Prevention of Lower Respiratory Tract Disease Caused by The respiratory syncytial virus (RSV) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000630-17 | Sponsor Protocol Number: MER-XMT-1536-1 | Start Date*: 2021-09-21 | ||||||||||||||||
Sponsor Name:Mersana Therapeutics, Inc. | ||||||||||||||||||
Full Title: A Phase 1b/2, First-in-Human, Dose Escalation and Expansion Study of XMT-1536 In Patients with Solid Tumors Likely to Express NaPi2b | ||||||||||||||||||
Medical condition: High grade serous ovarian cancer or non-small cell lung cancer (NSCLC), adenocarcinoma subtype | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) NO (Completed) LT (Completed) CZ (Completed) HU (Completed) BG (Completed) FI (Completed) PL (Completed) DK (Completed) IT (Completed) AT (Completed) BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005924-16 | Sponsor Protocol Number: M13-377 | Start Date*: 2012-06-13 | |||||||||||
Sponsor Name:Abbott Laboratories Ireland Limited | |||||||||||||
Full Title: A 12-week, Double-blind, Randomized Study to Compare the Efficacy and Safety of Fixed Combinations of Fenofibrate /Simvastatin 145/20mg and Fenofibrate / Simvastatin 145/40mg Tablets vs. Matching M... | |||||||||||||
Medical condition: Dyslipidemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020855-29 | Sponsor Protocol Number: E1496/09 | Start Date*: 2009-10-16 | ||||||||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI MESSINA | ||||||||||||||||||
Full Title: Radioiodine ablation of post-surgical thyroid remnants by recombinant human TSH (rhTSH) in patients with moderately severe and severe Graves' orbithopathy (GO) | ||||||||||||||||||
Medical condition: Patients affected with moderately severe and severe GO | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001015-14 | Sponsor Protocol Number: VAC18195RSV1001 | Start Date*: 2022-10-05 |
Sponsor Name:Janssen Vaccines & Prevention B.V. | ||
Full Title: A Randomized, Double-blind, Placebo-controlled Phase 1/2a Study for Safety and Immunogenicity Evaluations of various RSV.preF-based Vaccine Formulations in Adults Aged 60 Years and Older | ||
Medical condition: Healthy volunteer (prevention of lower respiratory tract disease caused by respiratory syncytial virus (RSV)) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-001825-33 | Sponsor Protocol Number: 61186372NSC3002 | Start Date*: 2021-10-27 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 3, Open-Label, Randomized Study of Amivantamab and Lazertinib in Combination with Platinum-Based Chemotherapy Compared with Platinum-Based Chemotherapy in Patients with EGFR-Mutated Locally... | |||||||||||||
Medical condition: Locally Advanced or Metastatic Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) DE (Trial now transitioned) PL (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) DK (Trial now transitioned) BG (Trial now transitioned) PT (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001810-13 | Sponsor Protocol Number: GSN000350 | Start Date*: 2021-12-11 | |||||||||||
Sponsor Name:Genkyotex Suisse SA | |||||||||||||
Full Title: TRANSFORM: A 52-week, Randomized, Placebo controlled, Double blind, Adaptive Phase 2b/3 Trial of Setanaxib with a 52 week Extension Phase in Patients with Primary Biliary Cholangitis (PBC) and Elev... | |||||||||||||
Medical condition: Primary Biliary Cholangitis (PBC) and Elevated Liver Stiffness | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) AT (Completed) FR (Completed) ES (Prematurely Ended) PL (Completed) IT (Completed) GR (Completed) SE (Completed) CZ (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003279-23 | Sponsor Protocol Number: MOMEL27 | Start Date*: 2020-01-13 |
Sponsor Name:Radboudumc | ||
Full Title: Phase 2 Study testing the COmbination of Vemurafenib With Cobimetinib in BRAF V600 mutated Melanoma Patients to Normalize LDH and Optimize immunotherapY with Nivolumab and Ipilimumab (COWBOY) | ||
Medical condition: Stage IV or unresectable stage III, BRAFV600E/K mutation positive melanoma, naïve for BRAF/MEK, PD-1/PD-L1 or CTLA-4 targeting therapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000004-42 | Sponsor Protocol Number: C0993 | Start Date*: 2019-01-16 | |||||||||||
Sponsor Name:The Clatterbridge Cancer Centre NHS Foundation Trust | |||||||||||||
Full Title: TACE-3: A two-arm multi-stage (TAMS) seamless phase II/III randomised trial of nivolumab in combination with TACE/TAE for patients with intermediate stage HCC | |||||||||||||
Medical condition: Intermediate stage Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003080-31 | Sponsor Protocol Number: 172003 | Start Date*: 2006-12-12 | |||||||||||
Sponsor Name:NV Organon | |||||||||||||
Full Title: A multi-center, double-blind, flexible-dose efficacy trial with Org 25935 versus placebo as add-on therapy in subjects with predominant, persistent negative symptoms of schizophrenia treated with a... | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) FI (Completed) FR (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002874-30 | Sponsor Protocol Number: 008424QM | Start Date*: 2012-12-10 | |||||||||||
Sponsor Name:Queen Mary University of London | |||||||||||||
Full Title: AN OPEN LABEL RANDOMISED PHASE II STUDY COMPARING AZD2014 VERSUS EVEROLIMUS IN PATIENTS WITH ADVANCED METASTATIC RENAL CANCER AND PROGRESSION ON VEGF TARGETED THERAPY | |||||||||||||
Medical condition: Metastatic Clear Cell Renal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003586-41 | Sponsor Protocol Number: A6281289 | Start Date*: 2007-12-17 | |||||||||||
Sponsor Name:Pfizer Ltd. Ramsgate Road, Sandwich, Kent, CT13 9NJ, UK | |||||||||||||
Full Title: Placebo-controlled trial on the efficacy of growth hormone replacement therapy in patients with growth hormone deficiency after traumatic brain injury | |||||||||||||
Medical condition: Growth hormone deficiency after traumatic brain injury | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) SE (Prematurely Ended) GB (Prematurely Ended) FR (Prematurely Ended) ES (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018585-23 | Sponsor Protocol Number: A4061051 | Start Date*: 2010-12-21 | |||||||||||
Sponsor Name:Pfizer Inc 235 East 42nd Street, New York, NY10017 | |||||||||||||
Full Title: AG-013736 (axitinib) for the treatment of metastatic renal cell cancer (mRCC) | |||||||||||||
Medical condition: metastatic renal cell cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002598-49 | Sponsor Protocol Number: CRO1885 | Start Date*: 2012-04-23 |
Sponsor Name:Imperial College Joint Research Office | ||
Full Title: The AXitinib MicroBubble UltraSound in metastatic Colorectal cancer trial | ||
Medical condition: Third line colorectal liver metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000805-26 | Sponsor Protocol Number: PSYKFORSK_MAT-MDD | Start Date*: 2021-11-19 |
Sponsor Name:Østfold Hospital Trust | ||
Full Title: An Open-Label, Phase 2, Feasibility Study of Manualized MDMA-Assisted Psychotherapy in Subjects with Major Depressive Disorder | ||
Medical condition: Major Depressive Disorder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003963-20 | Sponsor Protocol Number: AIO-YMO/TRK-0416 | Start Date*: 2017-10-24 |
Sponsor Name:AIO-Studien-gGmbH | ||
Full Title: Durvalumab (MEDI4736) in frail and elder patients with metastatic NSCLC | ||
Medical condition: metastatic non-small cell lung cancer (NSCLC) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001483-28 | Sponsor Protocol Number: VAC31518COV1001 | Start Date*: 2020-07-14 |
Sponsor Name:Janssen Vaccines & Prevention B.V. | ||
Full Title: A Randomized, Double-blind, Placebo-controlled Phase 1/2a Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of Ad26COVS1 in Adults Aged 18 to 55 Years Inclusive and Adults Aged 65 Ye... | ||
Medical condition: Healthy volunteers (Prevention of COVID-19) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002947-27 | Sponsor Protocol Number: SIMCODE | Start Date*: 2020-01-22 |
Sponsor Name:Charité – Universitätsmedizin Berlin | ||
Full Title: Simvastatin add-on to Escitalopram in patients with comorbid obesity and major depression: A multicenter, randomized, double-blind, placebo-controlled trial | ||
Medical condition: Patients with comorbid obesity (body mass index ≥ 30) and major depression | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
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